HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296598Generated: October 30, 2026
5,6-Diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil → HCID 178456519, compound
https://huagongshe.com/reaction/1296598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5,6-Diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil | HCID 11609665 | — |
| Reactant | HCID 178525261 | HCID 178525261 | — |
| Product | HCID 178456519 | HCID 178456519 | — |
Reaction Steps
By the method of Example 2, 1H-tetrazole-5-acetic acid is reacted with 5,6-diamino-1-[2-(4-nitrophenyl)ethyl]-3-propyluracil (6) to yield 3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine. By the method of Example 3, this substance is alkylated with a mixture of 1,2-dichloroethane, sodium carbonate, and ethylamine to yield 7-(2-ethylamino)ethyl-3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine. By the method of Example 4,7-(2-ethylamino)ethyl-3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine is reduced with hydrazine hydrate or hydrogen gas in the presence of a palladium catalyst to yield 3-[2-(4-aminophenyl)ethyl]-7-(2-ethylamino)ethyl-1-propyl-8-[(1H-tetrazol-5-yl)methyl]xanthine free base. The corresponding hydrochloride salt is then made on exposure to an excess of hydrogen chloride in solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07247639B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-6b761e28d56f4c62ac4f26ccdd9c4751 |
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| Source note | uspto-grants-2007_07 |
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